1.Research development of heterogeneous extracellular matrix
Jile FU ; Shaojun LUO ; Jie LIANG
International Journal of Biomedical Engineering 2006;0(06):-
Extracellular matrix(ECM) is the research focus in organize engineering, The configuration?component and mechanics enviroment of ECM is fit for the growth and metastasis of the cell. Heterogeneous ECM is not widely used in clinical treatment for immunocompetence and ethics. This paper introduces the production?organize configuration? immunocompetence and the clinical application of heterogeneous ECM.
2.Serum epidemiological analysis of community patients with hepatitis B
Ximei GAO ; Yajie LIN ; Jing WANG ; Jile LIANG
Chinese Journal of Practical Nursing 2008;24(18):62-63
Objective To discuss and analyze the serum epidemiological characteristics of hepatitis B among people in Jinan in order to formulate applicable community nursing measures to control hepatitis B. Methods The serum marker of hepatitis B was tested by enzyme-linked immunosorbent assay in 26756 serum samples by strict operation according to the kit introduction. The data were analyzed by SPSS 13.0 software. Results The positive rate of HBsAg was 7.39%, among which the positive rate of male was 8.81% and female 5.54%, which was lower than that of the male (P<0.01). The positive rate of people lower than 20 years old was lower than those of above 20 years old. The positive rate of male from 21 to 30 years old was lower than those from 41 to 50 years old (P<0.05). No difference was seen between people with different professionals. Conclusions Vaccine inoculation of hepatitis B for susceptible population combined with community health education about hepatitis B related knowledge and comprehensive nursing intervention proved to be the pivotal measures for the control and prevention of hepatitis B.
3. Mutations in A(8) and A(9) loci of exon 8 of retinoblastoma protein-interacting zinc finger gene of keloid patients
Jile FU ; Gang ZHANG ; Jie LIANG ; Xuece MEI
Chinese Journal of Burns 2018;34(9):643-647
Objective:
To study the situation of the mutations in the A(8) and A(9) loci of exon 8 of retinoblastoma protein-interacting zinc finger gene (RIZ) of keloid patients.
Methods:
From January 2003 to December 2007, 19 outpatient and hospitalized keloid patients of our hospital were conforming to the inclusion criteria. Both 3-5 g keloid tissue and 3 mL peripheral venous blood were collected from each patient to extract their genomic DNA, and the concentration was determined. The A(8) and A(9) loci fragments of exon 8 of RIZ were amplified by polymerase chain reaction (PCR). The length of product was detected by agarose gel electrophoresis, and DNA sequencing was performed after column chromatography. The mutations of A(8) and A(9) loci fragments were searched, and the types of mutations were determined. The consistency of genetic mutations of the keloid tissue and peripheral venous blood were compared. Data were processed with McNemar test.
Results:
The DNA concentrations of the extracted keloid tissue and peripheral venous blood were 0.54 and 0.37 μg/μL, respectively, which were above 0.10 μg/μL. The lengths of PCR products of A(8) locus fragment DNA of exon 8 of RIZ from keloid tissue and peripheral venous blood were 235 and 238 bp, respectively, and those of A(9) locus were 242 and 244 bp, respectively, which were basically the same as the designed DNA fragments. PCR products purity of A(8) locus fragment DNA of exon 8 of RIZ from keloid tissue and peripheral venous blood were 1.81 and 1.75, respectively, and those of A(9) locus were 1.82 and 1.78, respectively, which were above 1.50. Mutations in the A(8) locus of exon 8 of RIZ were observed in keloid tissue of 18 patients, totally 6 gene mutations, including 4 point mutations and 2 frameshift mutations. Mutations in the A(9) locus of exon 8 of RIZ were observed in keloid tissue of 9 patients, totally 9 gene mutations, including 7 point mutations and 2 frameshift mutations. No patient had a mutation in the A(8) or A(9) locus of exon 8 of RIZ in peripheral venous blood. Compared with those of peripheral venous blood, the mutations in the A(8) and A(9) loci of exon 8 of RIZ in keloid tissue of patients were statistically significant (